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Biochemistry Endocrinology 1eac4f43

The enzyme defect in von Gierke&;s disease (type-1 glycogen storage disease) is

A
Glycogen phosphorylase
B
Debranching enzyme
C
Phosphoglucomutase
D
Glucose-6-phosphate
High-Yield Explanation
Von Gierke disease:DiseaseEnzyme deficiencyClinical featuresVon Gierke disease Glucose-6-phosphatase deficiencyGlycogen accumulation in liver and renal tubule cells; hypoglycemia; lactic acidemia; ketosis; hyperlipemiaReference: Harper&;s Biochemistry; 30th edition; Chapter 18; Metabolism of Glycogen
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